Ionic Liquids and Their Interaction with Cellulose - ACS Publications

Sep 16, 2009 - Introduction. Sustainability, industrial ecology, eco-efficiency, and green chemistry are directing the development of the next genera-...
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Chem. Rev. 2009, 109, 6712–6728

Ionic Liquids and Their Interaction with Cellulose Andre´ Pinkert,† Kenneth N. Marsh,*,† Shusheng Pang,† and Mark P. Staiger‡ Department of Chemical and Process Engineering and Department of Mechanical Engineering, University of Canterbury, Christchurch, New Zealand Received May 17, 2009

Contents 1. Introduction 2. Cellulose 3. Ionic Liquids 3.1. Fundamentals 3.2. Synthesis and Purification 3.3. Properties and Applications 3.3.1. Melting Temperature 4. Dissolution and Regenerating Cellulose 4.1. Introduction 4.2. Cellulose Dissolution Using Conventional Methods 4.3. Dissolution with Ionic Liquids 4.4. Regeneration of Cellulose 5. Functionalizing of Cellulose 6. Wood-Based Composites 6.1. Polymer Blends 6.2. All-Wood Composites 7. Conclusions and Remarks 8. Acknowledgments 9. Note Added after ASAP Publication 10. References

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1. Introduction Sustainability, industrial ecology, eco-efficiency, and green chemistry are directing the development of the next generation of materials, products, and processes. Biodegradable plastics and biocompatible composites generated from renewable biomass feedstock are regarded as promising materials that could replace synthetic polymers and reduce global dependence on fossil fuel sources.1 It is estimated that the world is currently consuming petroleum at a rate 100 000 times faster than nature can replace it.2 The growing global environmental awareness and societal concern, high rate of depletion of petroleum resources, concepts of sustainability, and new environmental regulations have triggered the search for new products and processes that are more compatible with the environment. The most abundant natural polymer in our environment is cellulose. It has an estimated annual biosphere production of 90 × 109 metric tons and, consequently, represents the most obvious renewable resource for producing biocomposites.3 Its highly ordered structure is responsible for its desirable mechanical properties but makes it a challenge to find suitable solvents for its dissolution.4 * To whom correspondence should be addressed. E-mail: ken.marsh@ canterbury.ac.nz. Tel.: +64 3364 2140. Fax: +64 3364 2063. † Department of Chemical and Process Engineering. ‡ Department of Mechanical Engineering.

Andre´ Pinkert was born in Schwabach, Germany, in 1981. He studied Chemistry at the University of Erlangen-Nu¨rnberg, Germany, and received his prediploma and diploma degrees in 2004 and 2008, respectively. During 2005, he joined the Marine Natural Products Group, lead by Murray H. Munro and John W. Blunt, at the University of Canterbury (UoC), New Zealand, working on the isolation and characterization of bioactive metabolites. In early 2006, he returned to Germany and resumed his studies at the University of Erlangen-Nu¨rnberg, finishing his degree under the supervision of Rudi van Eldik. Associated with his studies, during 2007, he worked for AREVA NP on radio-nuclear chemistry and computer modeling. Since 2008, he is studying towards a Ph.D. degree at UoC under the supervision of Shusheng Pang, Ken Marsh, and Mark Staiger. His research focuses on biocomposites from natural fibers, processed via ionic liquids.

The first attempts to dissolve cellulose date back to the early 1920s.5 Several aqueous and nonaqueous cellulose solvents have been discovered since then, but all of these solvents suffer either from high environmental toxicity or from insufficient solvation power.6 In general, the traditional cellulose dissolution processes require relatively harsh conditions and the use of expensive and uncommon solvents, which usually cannot be recovered after the process.6-10 However, a new class of solvents was opened to the cellulose research community, when in 2002 Swatloski et al. reported the use of an ionic liquid as solvent for cellulose both for the regeneration of cellulose and for the chemical modification of the polysaccharide.7 In 1934, Graenacher had discovered a solvent system with the ability to dissolve cellulose, but this was thought to be of little practical value at the time.11,12 Ionic liquids are a group of salts that exist as liquids at relatively low temperatures ( [BF4]- > [Tf2N]-. Density. Density is one of the most often reported properties of ILs, probably because nearly every application requires knowledge of density. In general, ionic liquids are denser than water. The molar mass of the anion significantly affects the overall density of ILs.50 The bis(methanesulfonyl)amide [Ms2N]- salts, for example, have lower densities than the [Tf2N]- salts. Given that the molar volumes of both anions are similar, this is due to the greater mass of the fluorinated [Tf2N]- anion.51 In addition, the packing may become more efficient as the alternating positive and negative ions are of similar size.50 Surface Tension. Little data has been published on the surface tension of ILs.48,49 In general, the liquid/air surface tensions of ILs are somewhat higher than conventional solvents, except for water, and span an unusually wide range.50 Surface tension values vary with temperature, and both the surface excess entropy and energy are affected by the alkyl chain length, decreasing with increasing chain length. For a specific cation, the compound with the larger anion has, in general, the higher surface tension.52 However, alkylimidazolium [PF6]- salts have a higher surface tension than the corresponding [Tf2N]- salts.50 Thermal Stability. Most ILs exhibit relatively high thermal stability, with onset decomposition temperatures (Tonset) of (300 to 400) °C. The decomposition appears to be independent of the cation but decreases as the hydrophilicity of the anion increases.50 In general, it has been suggested that the stability dependence on the anion is [PF6]- > [Tf2N]≈ [BF4]- > X-.53 However other factors can affect the thermal stability. Fluorinated anions such as [PF6]- and

Ionic Liquids and Their Interaction with Cellulose

[BF4]-, for example, are unstable in the presence of water and decompose to produce HF.28,31,54 In thermogravimetric analysis (TGA), some metals catalyze decomposition; hence, it is advisable to use sample pans made of platinum rather than aluminum.53,55 The thermal stability of ILs has been revised recently as it was shown that degradation occurs at much lower temperatures if the temperature is held at that elevated level for a longer period (≈10 h). On the basis of these observations, the introduction of a new parameter describing the maximum operating temperature without degradation is suggested.55,56 The anions usually decompose via dealkylation, whereas the cations undergo primarily alkyl migration and elimination reactions.55 In general, imidazolium salts tend to be more stable than tetraalkylammonium salts.53 Polarity. For molecular solvents, the term “polarity” is often related to its ability to dissolve other compounds. The precise definition of “solvent polarity” is complex since this term encompasses many molecular properties responsible for interactions between solvent and solute molecules (e.g., Coulombic, directional, inductive, dispersion, hydrogen bonding, electron pair donor, and electron pair acceptor forces). Hence, the quantitative characterization of “solvent polarity” remains a problem not completely solved for molecular solvents.50 The most common method to describe the polarity of ionic liquids is the solvatochromic determination of the Kamlet-Taft parameters. Fluorescence spectra, refractive indices, or organic reactions have been also used to determine polarity.57,58 The linear solvation-energy relationship (LSER) parameters are empirical and attempt to describe both H-bond basicity/acidity and polarity/polarizability. As a rule of thumb, ILs are polar solvents similar to short- to medium-chain alcohols.57,58 Water impurities do not greatly influence the polarity. Anions have the greatest effect on the H-bond basicity, and the polarity of ILs depend to some extent on the polarity of their environment.59,58 Permittivity. The relative dielectric permittivity, previously known as dielectric constant εs, cannot be used for the quantitative characterization of solvent polarity as this property does not provide an adequate correlation with much of the experimental data of molecular solvents. Conventional methods for measurement of εs are not applicable due to the high electrical conductivity of ionic liquids, although measuring the permittivity at high frequencies (f > 5 GHz) and subsequent extrapolation to zero frequency provides an estimate of the relative permittivities.60-63 Huang and Weingaertner conclude that the relative permittivities of 1,3dialkylimidazolium ILs at ambient temperature vary little (εs ) 10 to 15) compared to that of molecular solvents. Even though εs of ILs can range from about 11 to 57, εs of ILs are significantly lower than those of common polar solvents.60,61 The influence of the anion on εs appears to be minor, and H-bonding influences the permittivity, and hence the polarity, in very much the same way as in molecular liquids.61 Table 1 tests the relative dielectric permittivity and the cellulose dissolving power of some ILs. Molten salts with fluoride-containing anions are poor cellulose solvents and also have low permittivities. In contrast, 2-hydroxyethylammonium formate [HEA]Fmt displays the highest permittivity measured for an IL so far, and it also possesses high cellulose-dissolving ability.61 The relationship between per-

Chemical Reviews, 2009, Vol. 109, No. 12 6717 Table 1. Cellulose-Dissolving Capacity of Ionic Liquids in Mass Fraction (w) in Correlation to Their Relative Dielectric Permittivity

ionic liquida [HEA]Fmt [EMIM]EtOSO3 [EMIM]BF4 [EMIM]Tf2N [BMPyr]Tf2N [BMIM]BF4 [BMIM]PF6

relative dielectric cellulose solubility permittivity at 20 °C 100 w 30 0 0 0 0 0 0

57.3 27.9 12.9 12.3 11.7 11.7 11.4

references cellulose solubility/ permittivity Bicak65/Huang61 Zavrel66/Weingaertner60 Zavrel66/Weingaertner60 Zavrel66/Weingaertner60,62 Zavrel66/Weingaertner63 Zavrel66/Weingaertner60 Zavrel66/Weingaertner60

a Cations: [HEA] ) 2-hydroxyethylammonium, [EMIM] ) 1-ethyl3-methylimidazolium, [BMIM] ) 1-butyl-3-methylimidazolium, [BMPyr] ) 1-butyl-3-methylpyrrolidinium. Anions: Fmt ) formate, BF4 ) tetrafluoroborate, PF6 ) hexafluorophosphate, Tf2N ) bis(trifluoromethanesulfonyl)amide, EtOSO3 ) Ethylsulfate.

mittivity and cellulose-dissolving power of ionic liquids has yet to be systematically studied. Miscibility with Water. The hydrophilic/hydrophobic nature of ILs determines their solvation properties, which determines the recovery of products by solvent extraction and environmental contamination through wastewater. A recent publication indicates a route for separating watermiscible ILs from the aqueous phase.67 The miscibility of ILs with water depends mainly on the hydrophilic nature of the anion and the hydrophobic nature of the cation, which is primarily determined by the length of the alkyl chains.50 In general, the solubility of water decreases with a decrease in temperature. All ILs are hygroscopic to some extent and absorb water from the atmosphere. IR studies indicate that the water dissolved in ILs is mostly present in the “free” state, bonded via H-bonds to two anions. Cammarata et al. suggested that the degree of hydrophilicity of the IL can be used as an indicator for the strength of these H-bond interactions.68 Nuclear magnetic resonance (NMR) studies suggest that water molecules prefer to interact with the H-2, H-4, and H-5 protons of the imidazolium core and that the three-dimensional ion network of the ionic liquid is weakened as a result.69 Toxicity. Ionic liquids quickly gained attention as new solvents within the green chemistry community. Initially there were few environmental and ecological studies, and only within the last couple of years has the cytotoxic, environmental, and microbial toxicity of the most common ILs been studied.32,70-72 The effect of [BMIM]Cl, as the most widely used IL, on marine algae, Vibrio fischeri, luminescent bacteria, leukemia cell lines, or enzymes like acetylcholinesterase (which plays an essential role in the nervous system of all higher organisms) showed that the IL was not acutely toxic (EC50 ≈ 13 µM).70 However, the toxicity of ILs increases dramatically with increase in the length of the alkyl side chain, due to an increase in lipophilicity. The cation dominates the toxic effect of ILs, although some influence of the anion has been shown.71 In general, imidazolium ILs are more toxic than the more bulky phosphonium ILs, and it is recommended to work with the shorter methyl side chain on the cation core (instead of ethyl) wherever possible.72,73 Currently there is a lack of in vivo investigations on IL biouptake. Life-cycle analysis of ILs with more emphasis on recycling has been proposed by the research community.71,72 Access of Thermophysical Properties. Easy access to the exponentially increasing rate of publications on ILs

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Pinkert et al.

Figure 10. Traditional cellulose solvents: N,N-dimethylacetamide/lithium chloride (DMA/LiCl), dinitrogen tetroxide/dimethylformamide (N2O4/DMF), N-methylmorpholine-N-oxide (NMMO), mineral acids, sodium hydroxide (NaOH), dimethylsulfoxide/tetrabutylammonium fluoride (DMSO/TBAF), dimethylimidazolone/lithiumchloride, molten salt hydrates.

during the past decade requires a comprehensive data collection of as many properties as possible.22 The most comprehensive data collection (1984 to 2004) of IL properties with 1680 property data compound combinations was published by Zhang et al. in 2006, prior to the establishment of the IUPAC operated, freely accessible online database “IL Thermo”.74 It is regularly updated and contains, at the time of writing, property data of 339 ionic liquids with a total number of 212 different ions and more than 20 000 property data points for pure ionic liquids.75 Mixture data is also included.

4. Dissolution and Regenerating Cellulose 4.1. Introduction Cost-effective and environmentally friendly dissolution of cellulose is crucial for advancing the use of the biopolymer in new materials such as wood composites. Ideally, all H-bonds within the cellulose microfibrils would be broken during the dissolution process. The dissolved polysaccharide could then be mixed with other biopolymers (lignin, hemicellulose, chitosan, keratin fibers, etc.) as reinforcements, before solvent recovery with the cellulose forming strong inter- and intramolecular H-bonds with itself and the other components. Molecular modeling of interfaces between cellulose and surrounding molecules suggest that the interfacial interactions are dominated by Coulomb interactions, predominantly by hydrogen bonds.21 In reality, it is difficult to dissolve cellulose because degradation of the glucosidic bonds of the single cellulose chains occurs under too drastic conditions, and sometimes the regenerated biopolymer does have a lower degree of polymerization (DP) than the initial starting material.76

4.2. Cellulose Dissolution Using Conventional Methods The efficient dissolution of cellulose is a long-standing goal in cellulose research and development and is still of great importance. Natural cellulose contains highly crystalline regions, and the highly branched H-bonding network makes it insoluble in water and many organic solvents. Figure 10 gives an overview of the most common traditional cellulose solvents.5,37,77-81 Depending on the interaction of the solvent molecules with the polysaccharide, these solvents are called derivatizing or nonderivatizing.83 Derivatizing solvents interact chemically with the cellulose hydroxyl groups and

form intermediates. Nonderivatizing solvents do not. Commercial examples for derivatizing cellulose solvents are sodium hydroxide/carbon disulfide (Viscose) or sodium hydroxide/urea (CarbaCell) mixtures.16,83 N-methylmorpholine-N-oxide monohydrate (NMMO) is used as a nonderivatizing solvent for direct dissolution of cellulose in industrial fiber-making (Lyocell process).84 A wider range of products and synthesis paths is available with the application of N,Ndimethylacetamide/LiCl and dimethylsulfoxide (DMSO)/ tetrabutylammonium fluoride trihydrate (TBAF), both nonderivatizing solvent systems.76,85 Recently, molten salt hydrates such as LiX · nH2O (X ) I-, NO3-, CH3CO2-, ClO4-) have been reinvestigated and shown to be efficient nonderivatizing solvents for cellulose.79 Studies on the chemical modification of the dissolved cellulose show that a rather large excess of reagent is necessary. This is due to the high water content of the salt hydrates, with the water being responsible for promoting unwanted side reactions.76 But most obvious from Figure 10 is that the very high polarity of these cellulose solvents, if not even ionic character, is favorable for the breakdown of the cellulose network. Furthermore, the chloride ion seems to be one of the favorite cellulose-dissolving anions; and although various mechanisms of the chloride-cellulose interactions have been proposed, no specific data is available to support these speculations.86

4.3. Dissolution with Ionic Liquids Ionic liquids appear to be highly polar due to their ionic character, resulting in their enhanced biopolymer dissolving capacity. Table 2 gives an overview of the cellulosedissolving capacity of ionic liquids reported in the literature. A number of factors influence the cellulose dissolution, and it is important to note that Table 2 deals only with the dissolution capacity of these solvents, and not with the kinetics. Low viscosity ILs promote the dissolution process (mainly due to the higher mobility of the ions), and longer dissolution times (>12 h) do not always lead to better results, especially at higher temperatures.87-89 The risk of partial degradation at elevated temperatures may count for the fact that the favored dissolution temperature is very often 10 °C above the melting point of the IL.76,90 Impressive results have been obtained when (3 to 5) s microwave pulses were used instead of thermal (external) heating. For example, the solubility of cellulose with a DP of 1000 could be increased by 150 %.7 Microwave heating

Ionic Liquids and Their Interaction with Cellulose

Chemical Reviews, 2009, Vol. 109, No. 12 6719

Table 2. Cellulose-Dissolving Capacity of Ionic Liquids and Other Solvents in Mass Fraction (w) for Different Degrees of Polymerization (DP) solution conditions a

b

ionic liquid

cellulose solubility 100w

DP (DP)

θ/°C

[BMIM]CF3SO3 [MMIM]MeSO4 [BMPy]Cl [BMPy]Cl [BMPy]Cl [BMPy]Cl H3PO4 [HEA]Fmt [IM]2AlxCly [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Cl [BMIM]Fmt [BMIM]Fmt [AMIM]Fmt NMMO NMMO [BMIM]Ac [EMIM]Ac [EMIM]Ac [EMIM]Ac [EMIM]Ac [EMIM]Ac [EMIM]Ac [EMIM]Ac [EMIM]Ac [EMIM]Cl [EMIM]Cl [EMIM]Cl [EMIM]Cl [EMIM]Cl [EMIM]Cl [AMIM]Cl [AMIM]Cl [AMIM]Cl [AMIM]Cl [AMIM]Cl [AMIM]Cl [AMIM]Cl

>50 >50 39 37 12 >5 38 30 25 25 11-25 ≈20 18 13.6 13.4 13 11 10 10 10 >10 8 8 7 >5 5 5 3 3 >3 >3 partiallysoluble 4 4 3 1 4 3 3 3 3 2 2 1.4 1.3-2.6 2 30 15 13.5 >5 >5 5 4 >30 14.5 14.5 12.5 11 10 10

Indulin AT (kraft lignin) Indulin AT (kraft lignin) 286 (172) 593 (412) 1198 (368) R-cellulose cellulose cellulose wood 1000 1175 n.a. 286 (307) 569 454 593 (544) (wool keratin fibers) 1198 (812) cellulose 1000 Indulin AT (kraft lignin) Norway spruce sawdust (wool keratin fibers) Norway spruce TMP R-cellulose Southern pine TMP 1000 1000 1000 maple wood flour wood chips wood chips n.a. n.a. n.a. n.a. wood wood wood lignin lignin lignin lignin lignin Southern yellow pine xylan 250 225 250 454 (444) 569 (537) 569 Indulin AT (kraft lignin) 225 569 R-cellulose spruce, beech, chestnut maple wood flour red oak Southern yellow pine 569 268 (329) cellulose 593 (580) R-cellulose 1198 (1129) Indulin AT (kraft lignin) 220 650 1085 250 250 1175

90 90 105 105 105 105 n.a. n.a. 110 microwave heating n.a. 100 83 n.a. n.a. 83 130 83 100 100 90 110 130 130 90 130 80 70 70 80 100-105 130 130 130 130 130 130 130 130 130 130 130 130 130 110 130 85 110 80 n.a. n.a. n.a. 90 110 n.a. 90 90 80 110 110 n.a. 90 100 90 90 90 90 80 80 n.a. 100 100 n.a.

t/h 24 24 12 12 12 12 n.a. 24 25 min n.a. 2 12 n.a. n.a. 12 10 12 5 mg/h n.a. 24 8 10 8 12 8 sonication n.a. n.a. 24 n.a. 15 8 27 4 4 4.5 10 21 3 2 27 4 8 16 8 n.a. n.a. n.a. n.a. n.a. n.a. 24 n.a. n.a. 12 12 24 16 16 n.a. 12 2 12 12 12 24 5 5 5 2 >3 >3 21.5 12.8 9 6 4 ≈3 12 4 4 10 6.8 >5 6 10 5 5 12 12 10 10 10 5 5 3 2 2 2 0.5 0.5